Variant report

Variant rs7119206
Chromosome Location chr11:58563883-58563884
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58562000-58572000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:58563600-58564000 Enhancers Fetal Brain Female brain
3 chr11:58563800-58564000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:58563800-58564200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr11:58563800-58564200 Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr11:58563800-58564200 Active TSS Brain Anterior Caudate brain
7 chr11:58563800-58564200 Bivalent/Poised TSS A549 lung
8 chr11:58563800-58564400 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr11:58563800-58564400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr11:58563800-58564400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr11:58563800-58564400 Enhancers Liver Liver

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